JPS62911B2 - - Google Patents
Info
- Publication number
- JPS62911B2 JPS62911B2 JP53153767A JP15376778A JPS62911B2 JP S62911 B2 JPS62911 B2 JP S62911B2 JP 53153767 A JP53153767 A JP 53153767A JP 15376778 A JP15376778 A JP 15376778A JP S62911 B2 JPS62911 B2 JP S62911B2
- Authority
- JP
- Japan
- Prior art keywords
- thf
- water
- methanol
- tetrahydrofuran
- alcohol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 168
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 123
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 83
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 61
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 57
- 238000004821 distillation Methods 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 21
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 16
- 150000001298 alcohols Chemical class 0.000 claims description 16
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 14
- 239000000203 mixture Substances 0.000 description 29
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 14
- 238000000895 extractive distillation Methods 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 8
- 238000000926 separation method Methods 0.000 description 8
- 238000010992 reflux Methods 0.000 description 7
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- -1 formyl acetals Chemical class 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000005416 organic matter Substances 0.000 description 4
- 238000010926 purge Methods 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- BSCHIACBONPEOB-UHFFFAOYSA-N oxolane;hydrate Chemical compound O.C1CCOC1 BSCHIACBONPEOB-UHFFFAOYSA-N 0.000 description 3
- BHIIWXJHALLFBD-UHFFFAOYSA-N oxolane;propan-2-ol Chemical compound CC(C)O.C1CCOC1 BHIIWXJHALLFBD-UHFFFAOYSA-N 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- ZRSDQBKGDNPFLT-UHFFFAOYSA-N ethanol;oxolane Chemical compound CCO.C1CCOC1 ZRSDQBKGDNPFLT-UHFFFAOYSA-N 0.000 description 2
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- GRWIABMEEKERFV-UHFFFAOYSA-N methanol;oxolane Chemical compound OC.C1CCOC1 GRWIABMEEKERFV-UHFFFAOYSA-N 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 238000007363 ring formation reaction Methods 0.000 description 2
- FVJPIFWJQUIPNO-UHFFFAOYSA-N 2-methylpropan-2-ol;oxolane Chemical compound CC(C)(C)O.C1CCOC1 FVJPIFWJQUIPNO-UHFFFAOYSA-N 0.000 description 1
- NRBLHMFKCQZNHY-UHFFFAOYSA-N 3-(5-methyl-1,3-dioxan-2-yl)propanal Chemical compound CC1COC(CCC=O)OC1 NRBLHMFKCQZNHY-UHFFFAOYSA-N 0.000 description 1
- REIDAMBAPLIATC-UHFFFAOYSA-N 4-methoxycarbonylbenzoic acid Chemical compound COC(=O)C1=CC=C(C(O)=O)C=C1 REIDAMBAPLIATC-UHFFFAOYSA-N 0.000 description 1
- QJQAWQSNMXLUDF-UHFFFAOYSA-N 5-methyl-1,3-dioxane Chemical compound CC1COCOC1 QJQAWQSNMXLUDF-UHFFFAOYSA-N 0.000 description 1
- 241000590810 Corades Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000039 congener Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/06—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
- C07D307/08—Preparation of tetrahydrofuran
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/860,788 US4175009A (en) | 1977-12-15 | 1977-12-15 | Separation of alcohol from tetrahydrofuran |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5488260A JPS5488260A (en) | 1979-07-13 |
| JPS62911B2 true JPS62911B2 (fr) | 1987-01-10 |
Family
ID=25334013
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15376778A Granted JPS5488260A (en) | 1977-12-15 | 1978-12-14 | Separation of alcohol from tetrahydrofuran |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4175009A (fr) |
| JP (1) | JPS5488260A (fr) |
| CA (1) | CA1116118A (fr) |
| DE (1) | DE2854312A1 (fr) |
| GB (1) | GB2010258B (fr) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2927931C3 (de) * | 1979-07-11 | 1982-03-11 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur kontinuierlichen Abtrennung von Methanol aus Mischungen von Tetrahydrofuran mit Methanol und Wasser |
| GB8717993D0 (en) * | 1987-07-29 | 1987-09-03 | Davy Mckee Ltd | Process |
| US5209825A (en) * | 1988-10-04 | 1993-05-11 | E. I. Du Pont De Nemours And Company | Preparation of purified concentrated BDO |
| GB8917864D0 (en) * | 1989-08-04 | 1989-09-20 | Davy Mckee London | Process |
| DE102004047201A1 (de) * | 2004-09-29 | 2006-03-30 | Basf Ag | Verfahren zur destillativen Aufarbeitung von Tetrahydrofuran |
| KR100700623B1 (ko) | 2005-12-07 | 2007-03-28 | 금호석유화학 주식회사 | 에틸렌글리콜을 이용한 공비혼합물의 분리방법 |
| KR100806672B1 (ko) | 2006-11-27 | 2008-02-26 | 금호석유화학 주식회사 | 부타디엔, 메틸알콜, 테트라하이드로퓨란 및 물이 함유된사이클로헥산 혼합물의 정제방법 |
| CN111943915B (zh) * | 2020-08-19 | 2024-03-29 | 上海立得催化剂有限公司 | 一种适用于聚烯烃催化剂生产企业的含醇的四氢呋喃溶液分离系统及其应用 |
| CN115197177A (zh) * | 2022-07-01 | 2022-10-18 | 扬州贝尔新环境科技有限公司 | 一种环保型四氢呋喃萃取精馏分离工艺 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2198651A (en) * | 1936-10-31 | 1940-04-30 | Celanese Corp | Organic compound |
| US2551626A (en) * | 1948-06-24 | 1951-05-08 | Standard Oil Dev Co | Separation of normal alcohols from branched chain alcohols |
-
1977
- 1977-12-15 US US05/860,788 patent/US4175009A/en not_active Expired - Lifetime
-
1978
- 1978-10-31 CA CA315,022A patent/CA1116118A/fr not_active Expired
- 1978-12-14 JP JP15376778A patent/JPS5488260A/ja active Granted
- 1978-12-15 DE DE19782854312 patent/DE2854312A1/de active Granted
- 1978-12-15 GB GB7848677A patent/GB2010258B/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB2010258A (en) | 1979-06-27 |
| CA1116118A (fr) | 1982-01-12 |
| DE2854312A1 (de) | 1979-06-21 |
| US4175009A (en) | 1979-11-20 |
| GB2010258B (en) | 1982-05-19 |
| JPS5488260A (en) | 1979-07-13 |
| DE2854312C2 (fr) | 1988-08-25 |
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